期刊文献+

轻度认知障碍患者痴呆转化预测的结构MRI纵向研究 被引量:10

Longitudinal structural MRI study in process of mild cognitive impairment converting to AD dementia
原文传递
导出
摘要 目的探讨轻度认知障碍(MCI)患者痴呆转化过程中结构MRI纵向变化特征以及基线期结构磁共振(sMRI)特征。方法收集自2009年9月至2011年3月就诊于首都医科大学宣武医院神经内科门诊及记忆专科门诊的MCI患者27例(MCI组),以及同期存各社区招募健康老年志愿者31例f正常对照组1,存基线期和随访期分别对其进行神经心理测评及sMRI影像数据采集,应用基于体素的形态学分析方法进行全脑灰质体积计算,根据随访期是否转化为AD将MCI组分为转化组(MCI—C组1(16例)和未转化组(MCI—nc组)(11例),比较3组受试者灰质体积的变化轨迹,并与神经心理测评结果进行相关性分析。结果(1)与MCI—nc组相比,MCI—c组存基线期双侧腹内侧前额叶、双侧额中回、双侧颞上回存在明显的脑萎缩;(2)正常对照组的萎缩程度明显低于其他2组,MCI—c组的萎缩范围及程度与MCI—nc组比较差异无统计学意义(p〉0.05);(3)MCI—c组受试者内侧颖叶、海码、海马旁叫、楔前叶、顶下小叶等脑区的灰质体积下降与MMSE、MoCA评分呈止相父。结论MCI—C与MCI—nc患者的脑萎缩模式没有本质的区别,内侧颞叶、海马、海马旁回、楔前叶、顶下小叶等脑区灰质体积下降可能成为预测MCI向AD转化的结构影像学标记物。 Objective To explore the longitudinally changed patterns in the structure of mild cognitive impairment (MCI) due to Alzheimer's disease (AD) during the process of converting to AD dementia and further investigate the structural features at the baseline of MCI converters with the purpose of finding the potential structure l biomarkers which may predict the conversion in a short term. Methods Twenty-seven patients with MCI, collected from September 2009 to March 2011, and 31normal controls (NC) were enrolled in this study; neuropsychological assessment and structural magnetic resonance imaging (sMRI) data were acquired respectively at baseline and follow-up. Voxel-based morphometry (VBM) was used to calculate the whole brain gray matter volume. According to the follow up results, patients were divided into MCI converters group (MCI-a, n=16) and MCI non-converters group (MCI-nc, n=11); the trajectory of longitudinal sMRI among the three groups was compared and the correlation between sMRI and neuropsychological assessment was analyzed. Results As compared with MCI-nc group, there was obvious brain atrophy in the bilateral ventromedial prefrontal cortices, bilateral middle frontal gyri and bilateral superior temporal gyri in the MCI-c group. In the comparison of trajectory of sMRI longitudinal changes in the three groups, the degree of brain atrophy in NC group was much lower than the other two groups, and there was no significant difference between MCI-c and MCI-nc group. There were positive correlations between scores of mini-mental state examination and Montreal cognitive assessment and decreased volume of gray matter in the medial temporal lobe, hippocampus, parahippocampal gyms, precuneus, inferior parietal lobule, lateral temporal lobe and dorsolateral frontal lobe. Conclusions No essential difference in the pattern of encephalatrophy is noted between MCI-c and MCI-nc groups. The decline of brain gray matter volume in medial temporal lobe, hippocampus, parahippocampal gyms, precune
出处 《中华神经医学杂志》 CAS CSCD 北大核心 2016年第4期384-390,共7页 Chinese Journal of Neuromedicine
基金 (1)国家自然科学基金(31371007、81430037)(2)北京市科委首都市民健康培育项目(Z131100006813022)(3)凯力康医学研究项目(201206006)
关键词 阿尔茨海默病 轻度认知障碍 纵向研究 磁共振成像 Alzheimer's disease Mild cognitive impairment Longitudinal study Magneticresonance imaging
  • 相关文献

参考文献18

  • 1Li X, Cao M, Zhang J, et al. Structural and functional brain changes in the default mode network in subtypes of amnestic mild cognitive impairment[J]. J Geriatr Psychiatry Neurol, 2014, 27(3): 188-198. DOI: 10.1177/0891988714524629. 被引量:1
  • 2Petersen RC. Mild cognitive impairment as a diagnostic entity[J]. J Intern Med, 2004, 256(3): 183-194. DOI: 10.1111/j.1365-2796.2004. 01388.x. 被引量:1
  • 3Albert MS, DeKosky ST, Dickson D, et al. The diagnosis of mild cognitive impairment due to Alzheimer's disease: recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease [J]. Alzheimers Dement, 2011, 7(3): 270-279. DOI: 10.1016/j.jalz. 2011.03.008. 被引量:1
  • 4Han Y, Wang J, Zhao Z, et al. Frequency-dependent changes in the amplitude of low-frequency fluctuations in amnestic mild cognitive impairment: a resting-state fMRI study[J]. Neuroimage, 2011, 55 (1): 287-295. DOI: 10.1016/j.neuroimage.2010.11.059. 被引量:1
  • 5Dubois B, Feldman HH, Jacova C, et al. Research criteria for the diagnosis of Alzheimer's disease: revising the NINCDS-ADRDA zriteria[J]. Lancet Neurol, 2007, 6(8): 734-746. DOI: 10.1016/ 1474-4422 (07)70178-3. 被引量:1
  • 6Song XW, Dong ZY, Long XY, et al. REST: a toolkit for :esting-state functional magnetic resonance imaging data 9rocessing [J]. PLoS One, 2011, 6 (9): e25031. DOI: 10.1371/journal.pone.0025031. 被引量:1
  • 7Ledberg A, Akerman S, Roland PE. Estimation of the probabilities of 3D clusters in functional brain images[J]. Neuroimage, 1998, 8 (2): 113-128. DOI: 10.1006/nimg.1998.0336. 被引量:1
  • 8Xia M, Wang J, He Y. BrainNet Viewer: a network visualization tool for human brain connectomics [J]. PLoS One, 2013, 8 (7): e68910. DOI: 10.1371/journal.pone.0068910. 被引量:1
  • 9Rozzini L, Vicini CB, Bertoletti E, et al. The importance of Alzheimer disease assessment scale-cognitive part in predicting progress for amnestic mild cognitive impairment to Alzheimer disease[J]. J Geriatr Psychiatry Neurol, 2008, 21(4): 261-267. DOI: 10.1177/0891988708324940. 被引量:1
  • 10Fermema-Notestine C, McEvoy LK, Hagler D J, et al. Structural neuroimaging in the detection and prognosis of pre-clinical and early AD [J]. Behav Neurol, 2009, 21 (1): 3-12. DOI: 10.3233/BEN-2009-0230. 被引量:1

二级参考文献33

  • 1Roman GC. The epidemiology of vascular dementia[A] //In: Hartmann A, Kuschinsky W, Hoyer S, eds. Cerebral ischemia and dementia[M]. Bedim:Springer-Vedag, 1991, 9-15. 被引量:1
  • 2Mckhann G, Drachman D, Folstein M, et al. Clinical diagnosis of Alzheimer's disease: report of N1NCDS-ADRDA work group under the auspices of the Department of Health and Human Services Task Forces on Alzheimer's disease[J]. Neurology, 1984, 34: 939-944. 被引量:1
  • 3Roman GC, Tatemichi TK, Erkinjuntti, et al. Vascular dementia: diagnostic criteria for research studies: report of the N1NDS-AIREN Intemational Workshop [J]. Neurology, 1993, 43 (3): 250-260. 被引量:1
  • 4Chung JA, Cummings JL. Neumbehavioral and neuropsychiatric symptoms in Alzheimer's disease: characteristics and treatment[J]. Neurol Clin, 2000, 18(4): 829-846. 被引量:1
  • 5Blennow K, de Leon M J, Zetterberg H. Alzheimer's disease [J]. Lancet, 2006, 368(9533): 387-403. 被引量:1
  • 6Hardy J, Selkoe DJ. The amyloid hypothesis of Alzheimer' s disease: progress and problems on the road to therapeutics [J]. Science, 2002, 297(5580): 353-356. 被引量:1
  • 7Thai IA, Kantarci K, Reiman EM, et al. The role of biomarkers in clinical trials for Alzheimer disease [J]. Alzheimer Dis Assoc Disord, 2006, 20(1): 6-15. 被引量:1
  • 8Haass C, Selkoe DJ. Soluble protein oligomers in neurodegeneration: lessons from the Alzheimer's amyloid β-peptide [J]. Nat Rev Mol Cell Biol, 2007, 8(2): 101-112. 被引量:1
  • 9Shankar GM, Li S, Mehta TH, et al. Amyloid-β protein dimers isolated directly from Alzheimer's brains impair synaptic plasticity and memory [J]. Nat Med, 2008, 14(8): 837-842. 被引量:1
  • 10Georganopoulou DG, Chang L, Nam JM, et al. Nanoparticle-based detection in cerebral spinal fluid of a soluble pathogenic biomarker for Alzheimer's disease [J]. Proc Natl Acad Sci U S A, 2005, 102 (7): 2273-2276. 被引量:1

共引文献17

同被引文献55

引证文献10

二级引证文献64

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部